Standard

Menopause (age at onset)

PRRC2A · rs1046089

Stands on its own. Nothing else here links to this position yet — but the page above is the point: what the research found, what each genotype means, and where it came from, in language you can read. Links to conditions, drugs and the senses appear automatically if we write them.

What each result means

A/A Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Menopause (age at onset) compared to the general population. (GWAS Catalog, Hum Mol Genet 2013, PMID:23307926)

A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Menopause (age at onset). (GWAS Catalog, Hum Mol Genet 2013, PMID:23307926)

G/G Published research associates this genotype with typical/baseline likelihood of Menopause (age at onset) — no copies of the reported risk allele. (GWAS Catalog, Hum Mol Genet 2013, PMID:23307926)

Source: GWAS Catalog, Hum Mol Genet 2013, PMID:23307926

Questions about rs1046089

What is rs1046089?

rs1046089 is a single position in the genome, in or near the PRRC2A gene. Published research associates it with menopause (age at onset). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs1046089 mean I will get this?

No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.

Where does the information about rs1046089 come from?

GWAS Catalog, Hum Mol Genet 2013, PMID:23307926. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

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